{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94582",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution.",
      "recall_number": "Z-2629-2024",
      "product_description": "Medline procedure packs containing Shenli syringes, labeled as follows:    1) CVC INSERT BUNDLE 16CM, Pack Number ECVC3260;   2) VANTEX 7FR 3L 20CM CVC BUNDLE US, Pack Number ECVC8045",
      "product_quantity": "1,679,067 units in total",
      "reason_for_recall": "Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.",
      "recall_initiation_date": "20240408",
      "center_classification_date": "20240828",
      "report_date": "20240904",
      "code_info": "1) ECVC3260, Lot Number 2018052950;  2) ECVC8045, Lot Number 2023110290",
      "more_code_info": ""
    }
  ]
}